@article{SchmidtRiemerKarras2013,
  author    = {Schmidt, Bernd and Riemer, Martin and Karras, Manfred},
  title     = {2,2 '-Biphenols via protecting group-free thermal or microwave-accelerated suzuki-miyaura coupling in water},
  series = {The journal of organic chemistry},
  volume    = {78},
  journal   = {The journal of organic chemistry},
  number    = {17},
  publisher = {American Chemical Society},
  address   = {Washington},
  issn      = {0022-3263},
  doi       = {10.1021/jo401398n},
  pages     = {8680 -- 8688},
  year      = {2013},
  abstract  = {User-friendly protocols for the protecting group-free synthesis of 2,2'-biphenols via Suzuki-Miyaura coupling of o-halophenols and o-boronophenol are presented. The reactions proceed in water in the presence of simple additives such as K2CO3, KOH, KF, or TBAF and with commercially available Pd/C as precatalyst. Expensive or laboriously synthesized ligands or other additives are not required. In the case of bromophenols, efficient rate acceleration and short reaction times were accomplished by microwave irradiation.},
  language  = {en}
}